Controlled fracture connections for stents

• US 8,961,585 B2
• Filed: 04/25/2006
• Issued: 02/24/2015
• Est. Priority Date: 04/25/2005
• Status: Active Grant

• Current Assignee: Covidien LP (Medtronic Plc)
• Original Assignee: Covidien LP (Medtronic Plc)
• Inventors: Ma, Jianlu, Khouengboua, Ott, Grafov, Alex
• Primary Examiner(s): Severson, Ryan
• Assistant Examiner(s): MILES, JONATHAN WADE
• Application Number:
  US11/912,616
• Publication Number:
  US 20090036970A1
• Time in Patent Office: 3,227 Days
• Field of Search: 623/1.11, 623/1.15, 623/1.16, 623/1.17, 623/1.18, 623/1.19, 623/1.2
• US Class Current: 623/1.15
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91525 within the whole structure different bands showing different meander characteristics, e.g. frequency or amplitude
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/9155 Adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2002/91591 Locking connectors, e.g. using male-female connections
• CPC Class Codes: A61F 2210/0004 bioabsorbable
• CPC Class Codes: A61F 2250/0071 breakable or frangible

Abstract

The invention provides for intra-luminal stents, especially stent having controlled fracture connection, as well as, methods of making and using the same. In one embodiment, a stent for implantation into a vessel has a plurality of annular segments collectively forming tubular shape, characterized by at least first and second adjacent annular segments each defined by a plurality of struts and at least one joint interconnecting respective struts of the first and second segments on a non-permanent basis.

Claims

1. A stent for implantation into a body vessel, the stent having a generally tubular shape with a circumference and extending along a longitudinal axis, the stent comprising:

a first segment having a plurality of struts disposed along a first portion of the longitudinal axis and arranged to define a plurality of peaks;

a second segment, adjacent the first segment, having a plurality of struts;

at least two independent temporary struts, each temporary strut extending between and directly connecting the first segment and the second segment and being designed to fracture during use of the stent; and

at least one strut extending between and directly connecting the first segment and the second segment being designed to remain intact during use of the stent.

2. The stent of claim 1, further comprising a plurality of first and second segments arranged in an alternating pattern along the longitudinal axis.

3. The stent of claim 2, wherein struts of a second segment interconnect cells from different first segments of the plurality of the first segments.

4. The stent of claim 3, wherein the different first segments interconnected by the struts of a second segment are offset about the circumference of the stent.

5. The stent of claim 3, wherein the different of the first segments interconnected by the struts of a second segment are offset about the longitudinal axis of the stent.

6. The stent of claim 2, wherein the struts forming the open cells of the second segment are disposed in an arc of less than 60 degrees about the circumference of the stent.

7. The stent of claim 1, wherein the plurality of struts of the second segment temporarily interconnect cells from different first segments of the plurality of the first segments.

8. The stent of claim 1, wherein the struts of the second segment expand independent of each other.

9. The stent of claim 1, wherein the struts forming the open cells of the second segment are disposed in an arc of less than 180 degrees about the circumference of the stent.

10. The stent of claim 1, wherein the struts of the second segment comprise a biodegradable material.

11. The stent of claim 1, wherein a first temporary strut is configured to detach from at least one of the first segment and the second segment when subjected to a first stress level, and wherein a second temporary strut is configured to detach from at least one of the first segment and the second segment when subjected to a second stress level, the first stress level being different from the second stress level.

12. The stent of claim 1, wherein at least one temporary strut is made from the group consisting essentially of adhesive glue and epoxy.

13. The stent of claim 1, wherein at least one of the temporary struts include a first interlocking portion and a second interlocking portion, the first interlocking portion configured to interlock with the second interlocking portion.

14. The stent of claim 13, wherein the first interlocking portion includes a male structure and wherein the second interlocking portion includes a female structure.

15. An expandable stent for implantation into a body vessel comprising:

a plurality of annular segments collectively forming a tubular shape having a circumference and extending along a longitudinal axis, first and second annular segments being disposed adjacent to each other along the longitudinal axis,

a plurality of independent connectors, each independent connector extending between and directly joining the first and second annular segments, one or more of the connectors being temporary connectors designed to fracture during use of the stent, and one or more of the connectors being permanent connectors designed to remain intact during use of the stent.

16. The stent of claim 15, including at least two temporary connectors extending between and directly joining the first and second annular segments.

17. The stent of claim 16, including at least two permanent connectors extending between and directly joining the first and second annular segments.

18. A stent for implantation into a body lumen, the stent comprising:

a plurality of first and second segments arranged in an interconnected alternating pattern to form a generally tubular shape with a circumference and extending along a longitudinal axis,

the first segments comprising a plurality of struts forming closed cells having peaks disposed about the circumference of the stent; and

the second segments comprising a plurality of struts, a plurality of connecting struts between the first segments and the second segments being designed to fracture during proper use,

a first connecting strut extending between and directly connecting the first and second segments, the first connecting strut being configured and dimensioned to fracture when subjected to a first threshold stress level, and a second connecting strut extending between and directly connecting the first and second segments, the second connecting strut being configured and dimensioned to fracture when subjected to a second threshold stress level, the first stress level being different from the second stress level.

19. The stent of claim 18, wherein the struts of the second annular segments expand independently of each other.

20. The stent of claim 18, wherein the plurality of struts of the second segments comprise a biodegradable material.

21. A method for placing a stent within a body lumen comprising the steps of:

providing a stent having a plurality of first and second segments arranged in an interconnected alternating pattern to form a generally tubular shape having a circumference, the first segments comprising a plurality of struts disposed about the circumference of the stent, the second segments comprising a plurality of struts, the stent having a plurality of independent connectors extending between and directly connecting the first and second segments;

positioning the stent within the body lumen with a delivery mechanism;

causing the stent to expand within the body lumen in a manner which enables the struts of the second segments to expand independent of each other and enables a proportion of the connectors between the first and second segments to fracture and enables a proportion of the connectors between the first and second segments to remain intact.